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SunScreen
SunScreen - 52675-030-15 - (Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide)
Drug Information of SunScreen
| Product NDC: | 52675-030 |
| Proprietary Name: | SunScreen |
| Non Proprietary Name: | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Active Ingredient(s): | 7.5; 2; 4; 2.5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunScreen
| Product NDC: | 52675-030 |
| Labeler Name: | Crown Products, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120514 |
Package Information of SunScreen
| Package NDC: | 52675-030-15 |
| Package Description: | 15 mL in 1 BOTTLE (52675-030-15) |
NDC Information of SunScreen
| NDC Code | 52675-030-15 |
| Proprietary Name | SunScreen |
| Package Description | 15 mL in 1 BOTTLE (52675-030-15) |
| Product NDC | 52675-030 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120514 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Crown Products, LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 2; 4; 2.5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
